GB1111050A - Mixtures of water-insoluble disazo dyestuffs and process for their manufacture - Google Patents
Mixtures of water-insoluble disazo dyestuffs and process for their manufactureInfo
- Publication number
- GB1111050A GB1111050A GB36258/66A GB3625866A GB1111050A GB 1111050 A GB1111050 A GB 1111050A GB 36258/66 A GB36258/66 A GB 36258/66A GB 3625866 A GB3625866 A GB 3625866A GB 1111050 A GB1111050 A GB 1111050A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dyestuffs
- acetoacetylamino
- water
- optionally substituted
- general formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title abstract 4
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 230000008878 coupling Effects 0.000 abstract 4
- 238000010168 coupling process Methods 0.000 abstract 4
- 238000005859 coupling reaction Methods 0.000 abstract 4
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 abstract 2
- 239000000975 dye Substances 0.000 abstract 2
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 abstract 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 abstract 1
- JAAGHUBILRENEC-UHFFFAOYSA-N 1h-benzo[g]indazole Chemical compound C1=CC2=CC=CC=C2C2=C1C=NN2 JAAGHUBILRENEC-UHFFFAOYSA-N 0.000 abstract 1
- LLQCHJGEDKLPOX-UHFFFAOYSA-N 2-ethoxy-1,3-benzothiazole Chemical compound C1=CC=C2SC(OCC)=NC2=C1 LLQCHJGEDKLPOX-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- MYONAGGJKCJOBT-UHFFFAOYSA-N benzimidazol-2-one Chemical compound C1=CC=CC2=NC(=O)N=C21 MYONAGGJKCJOBT-UHFFFAOYSA-N 0.000 abstract 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 abstract 1
- 239000012964 benzotriazole Substances 0.000 abstract 1
- 229910052801 chlorine Chemical group 0.000 abstract 1
- 239000000460 chlorine Chemical group 0.000 abstract 1
- 238000004040 coloring Methods 0.000 abstract 1
- 238000004043 dyeing Methods 0.000 abstract 1
- -1 heterocyclic radical Chemical group 0.000 abstract 1
- HGVIAKXYAZRSEG-UHFFFAOYSA-N n-(2,4-dimethylphenyl)-3-oxobutanamide Chemical compound CC(=O)CC(=O)NC1=CC=C(C)C=C1C HGVIAKXYAZRSEG-UHFFFAOYSA-N 0.000 abstract 1
- KYYRTDXOHQYZPO-UHFFFAOYSA-N n-(2-methoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC=CC=C1NC(=O)CC(C)=O KYYRTDXOHQYZPO-UHFFFAOYSA-N 0.000 abstract 1
- MOUVJGIRLPZEES-UHFFFAOYSA-N n-(4-chloro-2,5-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(NC(=O)CC(C)=O)=C(OC)C=C1Cl MOUVJGIRLPZEES-UHFFFAOYSA-N 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 239000000025 natural resin Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000000344 soap Substances 0.000 abstract 1
- 230000003381 solubilizing effect Effects 0.000 abstract 1
- 238000009987 spinning Methods 0.000 abstract 1
- 239000000057 synthetic resin Substances 0.000 abstract 1
- 239000004753 textile Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000001052 yellow pigment Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/02—Disazo dyes
- C09B35/039—Disazo dyes characterised by the tetrazo component
- C09B35/08—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl
- C09B35/10—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl from two coupling components of the same type
- C09B35/105—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl from two coupling components of the same type from two coupling components with reactive methylene groups
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S534/00—Organic compounds -- part of the class 532-570 series
- Y10S534/01—Mixtures of azo compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF0046907 | 1965-08-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1111050A true GB1111050A (en) | 1968-04-24 |
Family
ID=7101309
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB36258/66A Expired GB1111050A (en) | 1965-08-14 | 1966-08-12 | Mixtures of water-insoluble disazo dyestuffs and process for their manufacture |
Country Status (10)
Country | Link |
---|---|
US (1) | US3529984A (pt) |
AT (1) | AT268474B (pt) |
BE (1) | BE685522A (pt) |
CH (1) | CH494263A (pt) |
DE (1) | DE1544534B2 (pt) |
DK (1) | DK123660C (pt) |
ES (1) | ES330161A1 (pt) |
FR (1) | FR90694E (pt) |
GB (1) | GB1111050A (pt) |
NL (1) | NL153260B (pt) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4665163A (en) * | 1982-06-26 | 1987-05-12 | Hoechst Aktiengesellschaft | Diaryl pigments with improved heat stability obtained by coupling bis-diazotized diamines with acetoacetanilides |
US4894094A (en) * | 1986-09-05 | 1990-01-16 | Basf Lacke & Farben Aktiengesellschaft | Disazo compounds and formulations containing same |
GB2235694A (en) * | 1989-08-10 | 1991-03-13 | Ciba Geigy Ag | Continuous process for the preparation of disazo pigment mixtures |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1356253A (en) * | 1970-05-06 | 1974-06-12 | Ciba Geigy Uk Ltd | Azo pigment compositions |
US5191070A (en) * | 1989-08-10 | 1993-03-02 | Ciba-Geigy Corporation | Continuous process for the preparation of bisazo pigment mixtures |
US8034174B2 (en) | 2008-04-18 | 2011-10-11 | Sun Chemical Corporation | Diarylide yellow pigments |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE636919A (pt) * | 1962-09-18 | |||
GB1058017A (en) * | 1965-06-24 | 1967-02-08 | Gnii Orch Poluproductov I Kras | Method of manufacture of transparent yellow monoazo pigments |
-
0
- FR FR90694D patent/FR90694E/fr not_active Expired
-
1965
- 1965-08-14 DE DE1544534A patent/DE1544534B2/de active Pending
-
1966
- 1966-08-09 NL NL666611188A patent/NL153260B/xx not_active IP Right Cessation
- 1966-08-11 US US571703A patent/US3529984A/en not_active Expired - Lifetime
- 1966-08-11 ES ES0330161A patent/ES330161A1/es not_active Expired
- 1966-08-11 CH CH1157966A patent/CH494263A/de not_active IP Right Cessation
- 1966-08-12 DK DK416366AA patent/DK123660C/da active
- 1966-08-12 AT AT773866A patent/AT268474B/de active
- 1966-08-12 GB GB36258/66A patent/GB1111050A/en not_active Expired
- 1966-08-16 BE BE685522D patent/BE685522A/xx unknown
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4665163A (en) * | 1982-06-26 | 1987-05-12 | Hoechst Aktiengesellschaft | Diaryl pigments with improved heat stability obtained by coupling bis-diazotized diamines with acetoacetanilides |
US4894094A (en) * | 1986-09-05 | 1990-01-16 | Basf Lacke & Farben Aktiengesellschaft | Disazo compounds and formulations containing same |
GB2235694A (en) * | 1989-08-10 | 1991-03-13 | Ciba Geigy Ag | Continuous process for the preparation of disazo pigment mixtures |
GB2235694B (en) * | 1989-08-10 | 1992-06-24 | Ciba Geigy Ag | Process for the preparation of bisazo pigment mixtures |
Also Published As
Publication number | Publication date |
---|---|
BE685522A (pt) | 1967-02-16 |
DE1544534B2 (de) | 1974-08-22 |
US3529984A (en) | 1970-09-22 |
DK123660C (da) | 1972-12-04 |
FR90694E (pt) | 1968-04-05 |
DK123660B (pt) | 1972-07-17 |
DE1544534A1 (de) | 1969-07-10 |
NL6611188A (pt) | 1967-02-15 |
ES330161A1 (es) | 1967-09-16 |
AT268474B (de) | 1969-02-10 |
CH494263A (de) | 1970-07-31 |
NL153260B (nl) | 1977-05-16 |
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